Canonical Allele Identifier: CA448985173
Gene: H2AC9P HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.26233393G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.26233165G>C , CM000668.2:g.26233165G>C GRCh38
NC_000006.11:g.26233393G>C , CM000668.1:g.26233393G>C GRCh37
NC_000006.10:g.26341372G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000403259.1:n.44G>C